BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LINEAGE(R) DURAMER(R) ACETABULAR LINER

    MDR report key: 2073199 · Received April 29, 2011

    Report

    Report Number
    1043534-2011-00179
    Event Type
    Injury
    Date Received
    April 29, 2011
    Report Date
    March 27, 2011
    Manufacturer
    WRIGHT MEDICAL TECHNOLOGY, INC.
    Product Code
    LPH
    PMA / PMN Number
    K002149
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION: UNAVAILABLE FOR FOLLOW UP.THE COMPLAINT WAS REVIEWED AND ANALYSIS SHOWED NO TREND FOR (B)(4) LOT NO: 06347192. THE DEVICE HISTORY RECORD WAS REVIEWED. THE PRODUCT WAS NOT RETURNED. PRODUCT NOT AVAILABLE FOR EVALUATION. INCOMPLETE INFORMATION.

    Additional Manufacturer Narrative · 1

    INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. THE EVENT CODE IS ADDRESSED IN THE PACKAGE INSERT. ALTHOUGH SEVERAL ATTEMPTS HAVE BEEN MADE, NO MEDWATCH 3500 HAS BEEN RECEIVED FROM THE USER FACILITY. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE. THIS IS THE SAME EVENT AS 1043534-2011-00180, 00181.

    Description of Event or Problem · 1

    ALLEGEDLY REVISED DUE TO WEAR AND OSTEOLYSIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LINEAGE(R) DURAMER(R) ACETABULAR LINER HIP COMPONENT LPH WRIGHT MEDICAL TECHNOLOGY, INC. 06347192

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Hospitalization| R